IFNL2[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 57043	GRCh38/hg38 19q13.12-13.2(chr19:37319377-42738688)x3	ACP7, ACTMAP +514 more	Copy number gain	See cases	GPathogenic
Select item 780556	NM_172138.2(IFNL2):c.18T>C (p.Thr6=)	IFNL2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3108300	NM_172138.2(IFNL2):c.29C>A (p.Thr10Lys)	IFNL2 (T10K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780557	NM_172138.2(IFNL2):c.29C>T (p.Thr10Met)	IFNL2 (T10M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3108303	NM_172138.2(IFNL2):c.97G>C (p.Gly33Arg)	IFNL2 (G33R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285380	NM_172138.2(IFNL2):c.107C>T (p.Pro36Leu)	IFNL2 (P36L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600359	NM_172138.2(IFNL2):c.221G>A (p.Arg74Lys)	IFNL2 (R74K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777474	NM_172138.2(IFNL2):c.227A>G (p.His76Arg)	IFNL2 (H76R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2226883	NM_172138.2(IFNL2):c.280C>T (p.Arg94Cys)	IFNL2 (R94C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340933	NM_172138.2(IFNL2):c.314C>T (p.Thr105Met)	IFNL2 (T105M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362550	NM_172138.2(IFNL2):c.359T>G (p.Val120Gly)	IFNL2 (V120G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2328294	NM_172138.2(IFNL2):c.450G>T (p.Arg150Ser)	IFNL2 (R150S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344390	NM_172138.2(IFNL2):c.461G>A (p.Arg154His)	IFNL2 (R154H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769454	NM_172138.2(IFNL2):c.478T>C (p.Tyr160His)	IFNL2 (Y160H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3108302	NM_172138.2(IFNL2):c.482G>A (p.Arg161Gln)	IFNL2 (R161Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328251	NM_172138.2(IFNL2):c.523G>A (p.Glu175Lys)	IFNL2 (E175K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555265	NM_172138.2(IFNL2):c.554T>A (p.Leu185His)	IFNL2 (L185H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2428774	NM_172138.2(IFNL2):c.562C>T (p.Arg188Ter)	IFNL2 (R188*)	Single nucleotide variant (nonsense)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 782646	NM_172138.2(IFNL2):c.588G>A (p.Gly196=)	IFNL2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3062386	GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	SLC7A9, SNRPA +215 more	Copy number gain	not specified	GPathogenic
Select item 2424211	NC_000019.9:g.(?_39205089)_(40913839_?)dup	ACP7, ACTN4 +53 more	Duplication	not provided	GUncertain significance
Select item 1330177	GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	ACP7, ACTMAP +255 more	Copy number gain	Specific learning disability	GPathogenic
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 253452	GRCh37/hg19 19q13.12-13.2(chr19:37582250-41630908)x3	DPF1, DYRK1B +105 more	Copy number gain	See cases	GPathogenic

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Items: 27